During ICSE 2017, co-located with CPhI Worldwide, Hall 4, Booth 40F33 our experts will highlight our latest developments in pharmaceutical contract services
During ICSE / CPhI Worldwide 2017 discuss your challenges for the critical stages of development, chemistry, manufacturing and controls (CMC), marketing authorization and GMP manufacturing with our outsourcing experts at Booth 40F33. We provide a range of laboratory services (analysis, bioanalysis, method development and validation, formulation, ICH stability programs, impurity analysis, QC and release testing), auditing and regulatory consultancy services to support your organization. Find out more about our specialist expertise in inhalation drug product development, biopharmaceutical characterisation, potency and immunogenicity testing and extractables /leachables studies.
To review your outsourcing plans for the coming year and beyond for either individual projects, or contracts covering long term relationships, please book a meeting with our Intertek Pharmaceutical Services team. We offer a flexible set of contract types which can be applied to your needs. During the event, you can find out about some of our specialist capabilities or discuss specific projects that you would like to get started.
WEBINAR RECORDING: Outsourcing Stability Studies to Contract Laboratories: Optimising Success
WEBINAR RECORDING: Design of Biopharmaceutical Stability Studies
WHITE PAPER DOWNLOAD: Pharmaceutical Stability Contingency Storage and Disaster Recovery
BROCHURE DOWNLOAD: Intertek Pharmaceutical Services
BROCHURE DOWNLOAD: Biopharmaceutical Services
BROCHURE DOWNLOAD: Inhalation Product Development Services
BROCHURE DOWNLOAD: Intertek Stability Services
BROCHURE DOWNLOAD: Intertek Bioanalysis Services
BROCHURE DOWNLOAD: Intertek Elemental Analysis & Impurities
We invite you to Booth 40F33 to provide more information about our services:
Need help or have a question?